Hi
I'm completely new on this. I have managed to perform alignments with Bowtie and used Cisgenome software to visualice the reads. However I have separated two peaks were I should have only one. I have been told to extend the reads according to the size of the sequenced fragments. How can I do that?
I'm completely new on this. I have managed to perform alignments with Bowtie and used Cisgenome software to visualice the reads. However I have separated two peaks were I should have only one. I have been told to extend the reads according to the size of the sequenced fragments. How can I do that?